A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6903884



Internal ID9668894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:893283..893719hg38UCSC Ensembl
Outerchr7:932920..933356hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733675
Supporting Variants
SamplesSSM013
Known GenesGET4
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6903884
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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